Cas 151267-01-5,(1S,2S,3R,4R)-4-acetoxymethyl-2,3-isopropylidenedioxycyclopentane-1-methanol α-methoxy-α-trifluoromethylphenylacetate

151267-01-5

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Basic information

Product Name: (1S,2S,3R,4R)-4-acetoxymethyl-2,3-isopropylidenedioxycyclopentane-1-methanol α-methoxy-α-trifluoromethylphenylacetate
Synonyms: (1S,2S,3R,4R)-4-acetoxymethyl-2,3-isopropylidenedioxycyclopentane-1-methanol α-methoxy-α-trifluoromethylphenylacetate
CAS NO:151267-01-5
Molecular Formula:
Molecular Weight: 460.447
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1S,2S,3R,4R)-4-acetoxymethyl-2,3-isopropylidenedioxycyclopentane-1-methanol α-methoxy-α-trifluoromethylphenylacetate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,3R,4R)-4-acetoxymethyl-2,3-isopropylidenedioxycyclopentane-1-methanol α-methoxy-α-trifluoromethylphenylacetate(151267-01-5)
EPA Substance Registry System: (1S,2S,3R,4R)-4-acetoxymethyl-2,3-isopropylidenedioxycyclopentane-1-methanol α-methoxy-α-trifluoromethylphenylacetate(151267-01-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 151267-01-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 151267-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,6 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 151267-01:
(8*1)+(7*5)+(6*1)+(5*2)+(4*6)+(3*7)+(2*0)+(1*1)=105
105 % 10 = 5
So 151267-01-5 is a valid CAS Registry Number.

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151267-01-5Relevant academic research and scientific papers

Enantioselective route to key intermediates in the synthesis of carbocyclic phosphoribosyltransferase transition state analogues

Ahmadian, Mohammad,Khare, Naveen K.,Riordan, James M.,Klon, Anthony E.,Borhani, David W.

, p. 9899 - 9909 (2001)

The enantioselective preparation of key intermediates in the synthesis of transition state analogues of hypoxanthine-guanine phosphoribosyltransferase, (1S,2S,3R,4R)-4-acetoxymethyl-1-bromomethyl-2,3-isopropylidenedioxy-1- toluenesulfonamidocyclopentane (3a) and the 4-nitrobenzenesulfonamido analogue (3b), are described.

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